A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105386



Internal ID22014619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34390674..34390674hg38UCSC Ensembl
chr19:34881579..34881579hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384763
hg194763
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628438
Samples
Known GenesGPI
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105386
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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